Steatocystoma multiplex, oligodontia and partial persistent primary dentition associated with a novel keratin 17 mutation

British Journal of Dermatology

Volumn 161, Issue 6, 2009, Pages 1396-1398

  Gass, J K ^a   Wilson, N J ^b   Smith, F J D ^c   Lane, E B ^b,d   McLean, W H I ^c   Rytina, E ^a   Salvary, I ^e   Burrows, N P ^a  

^a ADDENBROOKE S HOSPITAL   (United Kingdom)

^b IMPERIAL CANCER RESEARCH FUND   (United Kingdom)

^c UNIVERSITY OF DUNDEE   (United Kingdom)

^d INSTITUTE OF MEDICAL BIOLOGY   (Singapore)

^e JAMES PAGET UNIVERSITY HOSPITALS NHS FOUNDATION TRUST   (United Kingdom)

Author keywords

Hypodontia; Keratin 17; Pachyonychia congenita; Steatocystoma multiplex

Indexed keywords

CYTOKERATIN 17;

ADOLESCENT; ARTICLE; CASE REPORT; DECIDUOUS TOOTH; DNA DETERMINATION; GENE MUTATION; HUMAN; HUMAN TISSUE; MALE; MICROSCOPY; OLIGODONTIA; PHENOTYPE; PRIORITY JOURNAL; SCALP HAIR; SEBACEOUS CYST; SIBLING; SINGLE NUCLEOTIDE POLYMORPHISM; SKIN BIOPSY; SKIN DEFECT; SYNDACTYLY;

ADOLESCENT; ANODONTIA; DENTITION, PRIMARY; HUMANS; KERATIN-17; MALE; MUTATION; PACHYONYCHIA CONGENITA; PEDIGREE;

EID: 72649096620     PISSN: 00070963     EISSN: 13652133     Source Type: Journal    
DOI: 10.1111/j.1365-2133.2009.09383.x     Document Type: Article

References (10)

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